STRIDEX
- Product NDC
- 10157-1070
- 11-digit product format
- 101571070
- Labeler code
- 10157
- Product ID
- 10157-1070_eb9d76fe-ae97-4cf4-9efe-95613109df1b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Stridex naturally clear
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Blistex inc
- Application
- part333
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-11-23
- Marketing end
- 0000-00-00
- Substance
- SALICYLIC ACID
- Active strength
- 0 g/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10157-1070-1 | STRIDEXNaturally Clear | 70 in 1 JAR | LIQUID | 70 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10157-1070 | STRIDEX NATURALLY CLEAR LIQUID [BLISTEX INC ] | 1 | Legacy NDC, 1 package rows | 20100111_b3a78318-293a-4869-b442-3b6a9965791f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10157-1070-1 | 10157107001 | 70 in 1 JAR | Historical |